Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3815652 0.925 0.160 7 33873792 intron variant C/T snv 0.19 3
rs4788172 0.925 0.120 16 29656932 regulatory region variant G/A snv 0.12 2
rs2072069 0.925 0.120 17 34357972 intron variant G/A snv 0.47 2
rs1052632
MR1
0.925 0.080 1 181051094 non coding transcript exon variant G/A;C snv 2
rs12596308 0.925 0.120 16 29679875 intron variant C/A;T snv 2
rs17842268 0.925 0.120 16 29672859 intron variant T/C snv 0.36 2
rs7932766 0.925 0.080 11 126292967 synonymous variant C/T snv 0.18 0.19 2
rs352142 0.925 0.120 3 52232366 intron variant A/C snv 7.5E-02 2
rs352143 0.925 0.120 3 52230891 synonymous variant T/C snv 0.17 0.23 2